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Properties and molecular identity of NMDA receptors at synaptic and non-synaptic inputs in cerebellar molecular layer interneurons

机译:小脑分子层间神经元突触和非突触输入处NMDA受体的性质和分子同一性

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N-methyl-D-aspartate receptors (NMDARs) in cerebellar molecular layer interneurons (MLIs) are expressed and activated in unusual ways: at parallel fibre (PF) synapses they are only recruited by repetitive stimuli, suggesting an extrasynaptic location, whereas their activation by climbing fibre is purely mediated by spillover. NMDARs are thought to play an important role in plasticity at different levels of the cerebellar circuitry. Evaluation of the location, functional properties and physiological roles of NMDARs will be facilitated by knowledge of the NMDAR isoforms recruited. Here we show that MLI-NMDARs activated by both PF and climbing fibre inputs have similar kinetics and contain GluN2B but not GluN2A subunits. On the other hand, no evidence was found of functional NMDARs in the axons of MLIs. At the PF-Purkinje cell (PF-PC) synapse, the activation of GluN2A-containing NMDARs has been shown to be necessary for the induction of long-term depression (LTD). Our results therefore provide a clear distinction between the NMDARs located on MLIs and those involved in plasticity at PF-PC synapses.
机译:小脑分子层中神经元(MLI)中的N-甲基-D-天冬氨酸受体(NMDAR)以不同的方式表达和激活:在平行纤维(PF)突触中,它们仅通过重复刺激募集,表明突触外位置,而其激活攀爬纤维纯粹是由溢出所介导的。 NMDAR被认为在小脑电路的不同水平上的可塑性中起重要作用。 NMDAR同工型的知识将有助于评估NMDAR的位置,功能特性和生理作用。在这里,我们显示由PF和攀岩纤维输入激活的MLI-NMDAR具有相似的动力学,并且包含GluN2B,但不包含GluN2A亚基。另一方面,在MLI轴突中未发现功能性NMDAR。在PF-Purkinje细胞(PF-PC)突触处,已证明含有GluN2A的NMDAR的激活对于诱导长期抑郁(LTD)是必需的。因此,我们的结果为位于MLI上的NMDAR与参与PF-PC突触的可塑性的NMDAR之间提供了明显的区别。

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